68 research outputs found
Polymerase I and Transcript Release Factor Regulates Lipolysis via a Phosphorylation-Dependent Mechanism
OBJECTIVE: Polymerase I and transcript release factor (PTRF) is a protein highly expressed in adipose tissue and is an integral structural component of caveolae. Here, we report on a novel role of PTRF in lipid mobilization. RESEARCH DESIGN AND METHODS: PTRF expression was examined in different adipose depots of mice during fasting, refeeding, and after administration of catecholamines and insulin. Involvement of PTRF during lipolysis was studied upon PTRF knockdown and overexpression and mutation of PTRF phosphorylation sites in 3T3-L1 adipocytes. RESULTS: PTRF expression in mouse white adipose tissue (WAT) is regulated by nutritional status, increasing during fasting and decreasing to baseline after refeeding. Expression of PTRF also is hormonally regulated because treatment of mice with insulin leads to a decrease in expression, whereas isoproterenol increases expression in WAT. Manipulation of PTRF levels revealed a role of PTRF in lipolysis. Lentiviral-mediated knockdown of PTRF resulted in a marked attenuation of glycerol release in response to isoproterenol. Conversely, overexpressing PTRF enhanced isoproterenol-stimulated glycerol release. Mass-spectrometric analysis revealed that PTRF is phosphorylated at multiple sites in WAT. Mutation of serine 42, threonine 304, or serine 368 to alanine reduced isoproterenol-stimulated glycerol release in 3T3-L1 adipocytes. CONCLUSIONS: Our study is the first direct demonstration for a novel adipose tissueāspecific function of PTRF as a mediator of lipolysis and also shows that phosphorylation of PTRF is required for efficient fat mobilization
Leptin-induced lipolysis opposes the tonic inhibition of endogenous adenosine in white adipocytes
The aim of the present study was to gain insight into the signaling pathway used
by leptin to stimulate lipolysis. The lipolytic rate of white adipocytes from
sex- and age-matched lean (+/+) and fa/fa rats was determined in the absence or
presence of leptin together with a number of agents acting at different levels of
the signaling cascade. Leptin did not modify FSK-, dbcAMP-, and IBMX-stimulated
lipolysis. Lipolysis can also be maximally stimulated by lowering media adenosine
levels with adenosine deaminase (ADA), i.e., in the ligand-free state. Although
ADA produced near maximal lipolysis in adipocytes of lean animals, only half of
the maximal lipolytic rate (50.9+/-3.2%) was achieved in fat cells from fa/fa
rats (P=0.0034). In adipocytes from lean animals preincubated with ADA, leptin
caused a concentration-related stimulation of lipolysis (P=0.0001). However,
leptin had no effect on the lipolytic activity of adipocytes in the ligand-free
state from fa/fa rats. The adenosine A1 receptor agonist CPA effectively
inhibited basal lipolysis in both lean and obese adipocytes (P=0.0001 and
P=0.0090, respectively). Leptin had no effect on the lipolytic rate of adipocytes
isolated from fa/fa rats and preincubated with CPA. When adipocytes were
incubated with the A1 receptor antagonist DPCPX, a significant increase in
glycerol release was observed in fa/fa fat cells (P=0.009), whereas cells
isolated from lean rats showed no differences to ADA-stimulated lipolysis. After
pretreatment with PTX, which inactivates receptor-mediated Gi function,
adipocytes of obese rats became as responsive to the stimulatory actions of ISO
as cells from lean rats (P=0.0090 vs. ISO in fa/fa rats; P=0.2416 vs. lean rats,
respectively). PTX treatment of lean cells, however, did not alter their response
to this lipolytic agent. It can be concluded that the lipolytic effect of leptin
is located at the adenylate cyclase/Gi proteins level and that leptin-induced
lipolysis opposes the tonic inhibition of endogenous adenosine in white
adipocytes
Enriched finite elements for initial-value problem of transverse electromagnetic waves in time domain
Atrial natriuretic peptide contributes to the physiological control of lipid mobilization in humans
Fat in flames: influence of cytokines and pattern recognition receptors on adipocyte lipolysis
Ā© 2015 the American Physiological Society. Adipose tissue has the largest capacity to store energy in the body and provides energy through the release of free fatty acids during times of energy need. Different types of immune cells are recruited to adipose tissue under various physiological conditions, indicating that these cells contribute to the regulation of adipose tissue. One major pathway influenced by a number of immune cells is the release of free fatty acids through lipolysis during both physiological (e.g., cold stress) and pathophysiological processes (e.g., obesity, type 2 diabetes). Adipose tissue expansion during obesity leads to immune cell infiltration and adipose tissue remodeling, a homeostatic process that promotes inflammation in adipose tissue. The release of proinflammatory cytokines stimulates lipolysis and causes insulin resistance, leading to adipose tissue dysfunction and systemic disruptions of metabolism. This review focuses on the interactions of cytokines and other inflammatory molecules that regulate adipose tissue lipolysis during physiological and pathophysiological states
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